Variant report

Variant	nsv482597
Chromosome Location	chr19:43037214-43222644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2588)
CpG islands
(count:674)
Chromatin interactive
region (count:38)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2588 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:43071213-43071350	K562	blood:	n/a	n/a
2	ARID3A	chr19:43061956-43062073	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:43043390-43043643	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:43208643-43208644	K562	blood:	n/a	n/a
5	ATF1	chr19:43071854-43072090	K562	blood:	n/a	n/a
6	BACH1	chr19:43100672-43101041	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:43139260-43139326	K562	blood:	n/a	n/a
8	BACH1	chr19:43082922-43083098	K562	blood:	n/a	n/a
9	BACH1	chr19:43073712-43073803	K562	blood:	n/a	n/a
10	BACH1	chr19:43059655-43059806	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr19:43179178-43179402	GM12878	blood:	n/a	n/a
12	BATF	chr19:43132976-43133178	GM12878	blood:	n/a	chr19:43133094-43133104
13	BCL11A	chr19:43179101-43179287	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:43064904-43065169	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:43106732-43106880	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:43100628-43100974	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43138971-43139294	HepG2	liver:	n/a	n/a
18	BHLHE40	chr19:43071184-43071299	K562	blood:	n/a	n/a
19	BHLHE40	chr19:43139176-43139401	K562	blood:	n/a	n/a
20	BHLHE40	chr19:43071110-43071282	HepG2	liver:	n/a	n/a
21	BHLHE40	chr19:43064896-43065270	HepG2	liver:	n/a	n/a
22	BHLHE40	chr19:43064834-43065281	K562	blood:	n/a	n/a
23	BHLHE40	chr19:43110883-43111176	GM12878	blood:	n/a	n/a
24	BHLHE40	chr19:43110839-43111090	K562	blood:	n/a	n/a
25	BHLHE40	chr19:43067557-43067815	GM12878	blood:	n/a	n/a
26	BRCA1	chr19:43168346-43168356	GM12878	blood:	n/a	n/a
27	BRCA1	chr19:43111388-43111484	GM12878	blood:	n/a	n/a
28	CBX3	chr19:43190821-43191075	K562	blood:	n/a	n/a
29	CBX3	chr19:43188032-43188426	HCT-116	colon:	n/a	n/a
30	CBX3	chr19:43190865-43191064	K562	blood:	n/a	n/a
31	CBX3	chr19:43156238-43156476	K562	blood:	n/a	n/a
32	CEBPB	chr19:43156174-43156554	A549	lung:	n/a	chr19:43156349-43156360
33	CEBPB	chr19:43150294-43150473	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr19:43097919-43098273	A549	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
35	CEBPB	chr19:43067452-43067756	K562	blood:	n/a	n/a
36	CEBPB	chr19:43152306-43152361	IMR90	lung:	n/a	n/a
37	CEBPB	chr19:43128989-43129127	K562	blood:	n/a	n/a
38	CEBPB	chr19:43075958-43076158	A549	lung:	n/a	chr19:43076033-43076044
39	CEBPB	chr19:43043004-43043355	HepG2	liver:	n/a	chr19:43043164-43043175
40	CEBPB	chr19:43197904-43198224	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43110761-43111081	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:43127742-43127805	HepG2	liver:	n/a	chr19:43127762-43127773
43	CEBPB	chr19:43076011-43076056	HepG2	liver:	n/a	chr19:43076033-43076044
44	CEBPB	chr19:43067439-43067765	A549	lung:	n/a	n/a
45	CEBPB	chr19:43139258-43139346	K562	blood:	n/a	n/a
46	CEBPB	chr19:43156216-43156522	HepG2	liver:	n/a	chr19:43156349-43156360
47	CEBPB	chr19:43097951-43098246	HepG2	liver:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
48	CEBPB	chr19:43197922-43198219	A549	lung:	n/a	n/a
49	CEBPB	chr19:43071048-43071255	Hela-S3	cervix:	n/a	chr19:43071104-43071117
50	CEBPB	chr19:43045819-43046087	H1-hESC	embryonic stem cell:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43202122-43202172	SKMC	muscle:	n/a
2	chr19:43099845-43099895	HRE	kidney:	n/a
3	chr19:43202122-43202172	HRCEpiC	kidney:	n/a
4	chr19:43202122-43202172	SKMC	muscle:	n/a
5	chr19:43099845-43099895	HRE	kidney:	n/a
6	chr19:43202122-43202172	HRCEpiC	kidney:	n/a
7	chr19:43200890-43200940	NHDF-neo	bronchial:	n/a
8	chr19:43203368-43203418	AG04449	skin:	fetal
9	chr19:43202312-43202362	MCF-7	breast:	n/a
10	chr19:43198154-43198204	SK-N-MC	brain:	n/a
11	chr19:43099046-43099096	MCF10A-Er-Src	breast:	n/a
12	chr19:43085416-43085466	NHDF-neo	bronchial:	n/a
13	chr19:43202312-43202362	ovcar-3	ovarian:	n/a
14	chr19:43202312-43202362	CMK	blood:	n/a
15	chr19:43099845-43099895	HAEpiC	amniotic membrane:	n/a
16	chr19:43099124-43099174	SKMC	muscle:	n/a
17	chr19:43202312-43202362	HCF	heart:	n/a
18	chr19:43203368-43203418	PrEC	prostate:	n/a
19	chr19:43099795-43099845	ProgFib	skin:	n/a
20	chr19:43099845-43099895	NHBE	bronchial:	n/a
21	chr19:43200890-43200940	MCF-7	breast:	n/a
22	chr19:43099845-43099895	LNCaP	prostate:	n/a
23	chr19:43099124-43099174	ECC-1	luminal epithelium:	n/a
24	chr19:43202122-43202172	Hepatocyte	liver:	n/a
25	chr19:43099482-43099532	AG09319	gingival:	n/a
26	chr19:43085416-43085466	GM12878	blood:	n/a
27	chr19:43099124-43099174	H1-hESC	embryonic stem cell:	embryo
28	chr19:43099482-43099532	SK-N-SH	brain:	n/a
29	chr19:43099046-43099096	HCT-116	colon:	n/a
30	chr19:43203368-43203418	NH-A	brain:	n/a
31	chr19:43202122-43202172	AG04450	lung:	fetal
32	chr19:43099482-43099532	HepG2	liver:	n/a
33	chr19:43202122-43202172	A549	lung:	n/a
34	chr19:43202122-43202172	GM06990	blood:	n/a
35	chr19:43085416-43085466	AG09309	skin:	n/a
36	chr19:43085416-43085466	GM19239	blood:	n/a
37	chr19:43203368-43203418	T-47D	breast:	n/a
38	chr19:43099046-43099096	HRPEpiC	eye:	n/a
39	chr19:43085416-43085466	ovcar-3	ovarian:	n/a
40	chr19:43202122-43202172	BJ	skin:	n/a
41	chr19:43099845-43099895	K562	blood:	n/a
42	chr19:43198154-43198204	HCF	heart:	n/a
43	chr19:43202122-43202172	HCF	heart:	n/a
44	chr19:43099482-43099532	NHBE	bronchial:	n/a
45	chr19:43202122-43202172	NHBE	bronchial:	n/a
46	chr19:43099795-43099845	Hela-S3	cervix:	n/a
47	chr19:43200890-43200940	U87	brain:	n/a
48	chr19:43099046-43099096	HAEpiC	amniotic membrane:	n/a
49	chr19:43200890-43200940	HUVEC	blood vessel:	n/a
50	chr19:43085416-43085466	HUVEC	blood vessel:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
2	chr19:43139154..43139986-chr19:43246322..43246897,2	MCF-7	breast:
3	chr19:43068393..43071134-chr19:43075524..43077066,2	MCF-7	breast:
4	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
5	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
6	chr19:43070787..43071783-chr19:43100383..43100953,3	MCF-7	breast:
7	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
8	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:
9	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
10	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
11	chr19:42954441..42955205-chr19:43100309..43101289,2	MCF-7	breast:
12	chr19:42633464..42636070-chr19:43108015..43110975,2	K562	blood:
13	chr19:43149390..43151656-chr19:43158079..43159963,2	MCF-7	breast:
14	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
15	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
16	chr19:43068393..43071134-chr19:43075524..43077066,2	MCF-7	breast:
17	chr19:42965246..42967758-chr19:43079335..43081443,2	MCF-7	breast:
18	chr19:43070688..43071772-chr19:43100056..43100921,4	MCF-7	breast:
19	chr19:43092830..43095599-chr19:43097248..43100120,2	K562	blood:
20	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
21	chr19:43148558..43149434-chr20:53015100..53015659,2	MCF-7	breast:
22	chr19:43070787..43071783-chr19:43100383..43100953,3	MCF-7	breast:
23	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
24	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
25	chr19:42954317..42955251-chr19:43045554..43046465,4	K562	blood:
26	chr19:43068025..43070729-chr19:43097303..43100270,2	MCF-7	breast:
27	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
28	chr19:42954288..42955082-chr19:43045565..43046131,2	MCF-7	breast:
29	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
30	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
31	chr19:43070688..43071772-chr19:43100056..43100921,4	MCF-7	breast:
32	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
33	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
34	chr19:43067242..43067993-chr19:43100482..43101078,2	MCF-7	breast:
35	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
36	chr19:43067242..43067993-chr19:43100482..43101078,2	MCF-7	breast:
37	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
38	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066551
2	lnc-CEACAM8-1	chr19:43065825-43065902	NONHSAT066563
3	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066548
4	lnc-AC011497.1-2	chr19:43155869-43156816	NONHSAT066564
5	lnc-AC011497.1-2	chr19:43155239-43156171	ENSG00000213904.4
6	lnc-AC011497.1-2	chr19:43155388-43155602	NONHSAT066564
7	lnc-CEACAM8-1	chr19:43064585-43064946	NONHSAT066563
8	lnc-AC011497.1-2	chr19:43155239-43156507	ENSG00000213904.4

No data

Variant related genes	Relation type
CEACAMP1	TF binding region
RPS10P28	TF binding region
CEACAM8	TF binding region
CEACAMP5	TF binding region
CEACAM1	TF binding region
CEACAMP2	TF binding region
CEACAMP1	CpG island
RPS10P28	CpG island
CEACAM8	CpG island
CEACAMP5	CpG island
CEACAM1	CpG island
CEACAMP2	CpG island
ENSG00000231561	chromatin interactions
ENSG00000124469	chromatin interactions

Extended variants
information (count: 4978 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4978 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569868155	chr19:43037299-43037300	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs533455677	chr19:43037302-43037303	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs558685147	chr19:43037311-43037312	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs572465437	chr19:43037346-43037347	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs541116017	chr19:43037389-43037390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141090518	chr19:43037490-43037491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73932713	chr19:43037588-43037589	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs192636628	chr19:43037620-43037621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184760255	chr19:43037640-43037641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577489082	chr19:43037686-43037687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189216114	chr19:43037708-43037709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564735778	chr19:43037718-43037719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377118632	chr19:43037735-43037736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146907908	chr19:43037755-43037756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181562217	chr19:43037776-43037777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529881813	chr19:43037799-43037800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549733873	chr19:43037866-43037867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569888170	chr19:43037891-43037892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186930621	chr19:43037934-43037935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35811257	chr19:43037995-43037996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552487541	chr19:43038006-43038007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565935799	chr19:43038032-43038033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534723635	chr19:43038039-43038040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554625481	chr19:43038124-43038125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546563343	chr19:43038128-43038129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574605376	chr19:43038141-43038142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368193044	chr19:43038153-43038154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546722414	chr19:43038200-43038201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189782927	chr19:43038221-43038222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577425627	chr19:43038227-43038228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139383047	chr19:43038240-43038241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181220178	chr19:43038301-43038302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117832080	chr19:43038308-43038309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186096130	chr19:43038332-43038333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189916951	chr19:43038353-43038354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369676068	chr19:43038358-43038359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549909892	chr19:43038359-43038360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571613526	chr19:43038381-43038382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182172686	chr19:43038418-43038419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532381547	chr19:43038427-43038428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552164841	chr19:43038480-43038481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186454843	chr19:43038492-43038493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377758484	chr19:43038538-43038539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373667876	chr19:43038711-43038712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568169081	chr19:43038715-43038716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143292131	chr19:43038753-43038754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557468740	chr19:43038776-43038777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139715062	chr19:43038793-43038794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542653624	chr19:43038912-43038913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369563335	chr19:43038929-43038930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD

Chromatin state (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43033600-43038400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr19:43033600-43043000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:43033600-43043800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:43033600-43044200	Weak transcription	Gastric	stomach
5	chr19:43033800-43037600	Weak transcription	Liver	Liver
6	chr19:43033800-43038400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:43033800-43038600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr19:43033800-43039200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr19:43033800-43040000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr19:43033800-43043400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr19:43033800-43044200	Weak transcription	Brain Substantia Nigra	brain
12	chr19:43034000-43038400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr19:43034000-43038400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr19:43034000-43038600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr19:43034000-43039800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr19:43034000-43043000	Weak transcription	Adipose Nuclei	Adipose
17	chr19:43034200-43038400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr19:43034200-43038400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr19:43034200-43038400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr19:43034200-43043600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr19:43035200-43037600	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr19:43036800-43042800	Weak transcription	HMEC	breast
23	chr19:43037000-43037400	Enhancers	Brain Anterior Caudate	brain
24	chr19:43037000-43037600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr19:43037000-43037600	Enhancers	Brain Hippocampus Middle	brain
26	chr19:43037000-43038000	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr19:43037400-43039400	Weak transcription	Brain Anterior Caudate	brain
28	chr19:43037600-43039200	Weak transcription	Brain Hippocampus Middle	brain
29	chr19:43037600-43042800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr19:43038400-43038800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr19:43038400-43038800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr19:43038400-43038800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr19:43038400-43038800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr19:43038400-43038800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:43038400-43039000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr19:43038400-43039600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr19:43038400-43041000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr19:43038600-43038800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr19:43038800-43041400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr19:43038800-43043200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr19:43038800-43044000	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr19:43039000-43041200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr19:43039200-43040800	Enhancers	Brain Hippocampus Middle	brain
44	chr19:43039400-43039600	Enhancers	Brain Anterior Caudate	brain
45	chr19:43039400-43039600	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr19:43039800-43040400	Enhancers	Brain Cingulate Gyrus	brain
47	chr19:43040400-43044200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr19:43041000-43041400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr19:43041000-43043200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr19:43041400-43041600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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